ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2828474081
Gene: SCN2A
HGNC
NCBI
Linked Data
ClinVar Variation Id:
589983
ClinVar RCV Id:
RCV002318168
RCV002533055
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001358176.1:p.Asn308Ser
CA1939714
NM_001371247.1:c.923A>G